| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:125749426-125749748 | Common:5; Rare:127 | ||||
| chr6:125781059-125781121 | Rare:12 | ||||
| chr6:125986435-125986548 | Rare:44 | ||||
| chr6:127266767-127266910 | Common:2; Rare:61 | ||||
| chr6:127343343-127343399 | Rare:7 | ||||
| chr6:127343527-127343618 | Common:1; Rare:27 | ||||
| chr6:128520562-128520763 | Rare:76 | ||||
| chr6:128883032-128883362 | Common:2; Rare:89; Clinvar:8; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr6:132401420-132401615 | Common:1; Rare:59 | ||||
| chr6:133241042-133241387 | Common:5; Rare:102 | ||||
| chr6:133952907-133953238 | Common:2; Rare:84 | ||||
| chr6:134174788-134175121 | Common:1; Rare:168 | ||||
| chr6:135054745-135054913 | Common:3; Rare:51 | ||||
| chr6:135497618-135497888 | Common:4; Rare:99; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:136289779-136290006 | Common:1; Rare:97 |